Anna Rita Lizzi
University of L'Aquila
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Featured researches published by Anna Rita Lizzi.
Mini-reviews in Medicinal Chemistry | 2009
Anna Rita Lizzi; Veronica Carnicelli; Matilda Manuela Clarkson; Antonio Di Giulio; Arduino Oratore
Antimicrobial peptides, AMPs, exert their function acting mainly at the membrane level. In the wide AMPs panorama a particular position is occupied by lactoferrin derived peptides. They also possess antiviral, antifungal and antitumor activities and their parent molecules are available in several mammalian fluids and in dairy industries waste.
Biometals | 2004
Argante Bozzi; Fabrizia Brisdelli; Anna Maria D'Alessandro; Gabriele D'Andrea; Anna Rita Lizzi; Andrea C. Rinaldi; Arduino Oratore
Abstract3′-azido-3′-deoxythymidine (AZT), the first chemotherapeutic drug approved by FDA for treatment of HIV-infected patients and still used in combination therapy, has been shown to induce, upon prolonged exposure, severe bone marrow toxicity manifested as anemia, neutropenia and siderosis. These toxic effects are caused by inhibition of heme synthesis and, as a consequence, transferrin receptor (TfR) number appears increased and so iron taken up by cells. Since iron overload can promote the frequency and severity of many infections, siderosis is viewed as a further burden for AIDS patients. We have previously demonstrated that AZT-treated K562 cells showed an increase of the number of TfRs located on the surface of the plasma membrane without affecting their biosynthesis, but slowing down their endocytotic pathway. In spite of the higher number of receptors on the plasma-membrane of AZT-treated cells, intracellular accumulation of iron showed a similar level in control and in drug-exposed cells. The chelating ability of AZT and of its phosphorylated derivatives, both in an acellular system and in K562 cells, was also checked. The results demonstrated that AZT and AZTMP were uneffective as iron chelators, while AZTTP displayed a significant capacity to remove iron from transferrin (Tf). Our results suggest that AZT may be not directly involved in the iron overloading observed upon its prolonged use in AIDS therapy. The iron accumulation found in these patients is instead caused by other unknown mechanisms that need further studies to be clarified.
Molecular and Cellular Biochemistry | 2003
Gabriele D'Andrea; Anna Rita Lizzi; Fabrizia Brisdelli; Anna Maria D'Alessandro; Argante Bozzi; Arduino Oratore
AbstractIn this paper we report that 3
Food Chemistry | 2017
Alessandro Venditti; Claudio Frezza; Diana Celona; Armandodoriano Bianco; Mauro Serafini; Kevin Cianfaglione; Dennis Fiorini; Stefano Ferraro; Filippo Maggi; Anna Rita Lizzi; Giuseppe Celenza
Proteome Science | 2006
Gabriele D'Andrea; Anna Rita Lizzi; Sara Venditti; Laura Di Francesco; Alessandra Giorgi; Giuseppina Mignogna; Arduino Oratore; Argante Bozzi
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Biometals | 2011
Isabella Daidone; Alessandro Magliano; Alfredo Di Nola; Giuseppina Mignogna; Matilda Manuela Clarkson; Anna Rita Lizzi; Arduino Oratore; Fernando Mazza
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Cell Biochemistry and Function | 2017
Carla Luzi; Fabrizia Brisdelli; Roberto Iorio; Argante Bozzi; Veronica Carnicelli; Antonio Di Giulio; Anna Rita Lizzi
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Acta Biochimica et Biophysica Sinica | 2015
Veronica Carnicelli; Anna Rita Lizzi; G. Gualtieri; Argante Bozzi; Nicola Franceschini; Antonio Di Giulio
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Molecular and Cellular Biochemistry | 2007
Anna Rita Lizzi; Anna M D’Alessandro; Argante Bozzi; Benedetta Cinque; Arduino Oratore; Gabriele D’Andrea
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Biochemical Pharmacology | 2005
Anna Rita Lizzi; Anna M D’Alessandro; N. Zeolla; Fabrizia Brisdelli; Gabriele D’Andrea; G. Pitari; Arduino Oratore; Argante Bozzi; Rodolfo Ippoliti